Sogbein Olusola, Kochar Tina, Afrouzian Marjan
Department of Internal Medicine, Division of Nephrology and Hypertension, University of Texas Medical Branch, Galveston, Texas, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
Case Rep Nephrol. 2023 Jan 24;2023:3190042. doi: 10.1155/2023/3190042. eCollection 2023.
Membranous lupus nephritis associated with anti-GBM antibodies is a rare entity, particularly in lupus nephritis patients who are serologically negative for ANA and anti-dsDNA with normal complement levels. We present an unusual case of a patient initially diagnosed with anti-GBM disease whose repeat biopsy demonstrated combined focal proliferative and membranous lupus nephritis (III + V). The first biopsy showed a granular linear pattern, and the second biopsy had multiple electron dense deposits in the subendothelial, epithelial, and mesangial regions along with podocyte effacement. Experimental research suggests that the sequential histopathological transition observed may reflect the action of immunological rearrangement and epitope spreading.
与抗肾小球基底膜(GBM)抗体相关的膜性狼疮性肾炎是一种罕见的疾病,尤其是在抗核抗体(ANA)和抗双链DNA(anti-dsDNA)血清学阴性且补体水平正常的狼疮性肾炎患者中。我们报告了一例不寻常的病例,该患者最初被诊断为抗GBM病,其重复活检显示为局灶增生性和膜性狼疮性肾炎合并(III + V)。第一次活检显示为颗粒状线性模式,第二次活检在血管内皮、上皮和系膜区域有多个电子致密沉积物,伴有足细胞消失。实验研究表明,观察到的连续组织病理学转变可能反映了免疫重排和表位扩展的作用。